Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal thumb morphology (HP:0001172)

Grandparent Node:
Deviation of finger (HP:0004097)

Parent Node:
Deviation of the thumb (HP:0009603)

..Starting node
..Distally placed thumb (HP:0009622)

Term ID:

9622

Name:

Distally placed thumb

Synonym:

Definition:

Insertion of thumb at a more distal location than normal.

Comments:

Reference:

HP:0009622

Genes and Diseases:

Child Nodes:

Sister Nodes:

Clinodactyly of the thumb (HP:0040023)

Hitchhiker thumb (HP:0001234)

obsolete Radial deviation of the thumb (HP:0040021)

Proximal placement of thumb (HP:0009623)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009622	HP:0009622	Distally placed thumb	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.